Canonical Allele Identifier: CA367869961

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81355258G>C (hg19) ; chr7:g.81725942G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81725942G>C , CM000669.2:g.81725942G>C	GRCh38
NC_000007.13:g.81355258G>C , CM000669.1:g.81355258G>C	GRCh37
NC_000007.12:g.81193194G>C	NCBI36
NG_016274.1:g.49195C>G
NG_016274.2:g.49195C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.1116C>G MANE Select	ENSP00000222390.5:p.Ile372Met
ENST00000457544.7:c.1101C>G	ENSP00000391238.2:p.Ile367Met
ENST00000222390.9:c.1116C>G	ENSP00000222390.5:p.Ile372Met
ENST00000457544.6:c.1101C>G	ENSP00000391238.2:p.Ile367Met
NM_000601.4:c.1116C>G	NP_000592.3:p.Ile372Met
NM_001010932.1:c.1101C>G	NP_001010932.1:p.Ile367Met
XM_006715956.2:c.1116C>G	XP_006716019.1:p.Ile372Met
XM_011516115.1:c.1101C>G	XP_011514417.1:p.Ile367Met
NM_000601.5:c.1116C>G	NP_000592.3:p.Ile372Met
NM_001010932.2:c.1101C>G	NP_001010932.1:p.Ile367Met
XM_011516115.2:c.1101C>G	XP_011514417.1:p.Ile367Met
NM_000601.6:c.1116C>G MANE Select	NP_000592.3:p.Ile372Met
NM_001010932.3:c.1101C>G	NP_001010932.1:p.Ile367Met